Associate Manager, Source Configuration

As a Source Configuration Associate Manager on our Trial Design team, you will have the important responsibility of ensuring that clinical research professionals effectively and correctly collect, manage, and safeguard the very source data that demonstrate whether an investigational product is safe and effective. In streamlining our source configuration and administration process to ensure top-notch implementation of our products, you will have an impact on making clinical trials more efficient and cost effective, thereby reducing clinical research as a bottleneck that constrains the availability of new life-enhancing and life-saving treatments. Your clinical research experience, attention to detail, and ability to troubleshoot issues will be key as you ensure the success of multiple projects and/or teams within tight deadlines.

What You’ll Be Working On:

• Learn and maintain deep expertise in StudyTeam applications
• Review research protocols, CRF guidelines, and other stakeholder specifications to create accurate, comprehensive source form (CRF) templates
• Conduct and document thorough QA of source form templates
• Develop electronic forms, using Excel, from stakeholder specifications and feedback
• Build, test, and publish electronic source forms to maintain quality of the form designSupport and coordinate user acceptance testing 
• Collaborate with cross-functional teams to ensure successful execution of projects and provide feedback on product improvements to enhance our eSource product capabilities
• Develop, document, and implement best practices for standardization, QA, and process improvement around source form creation and digitization
• Provide mentorship, training, and support to more junior team members to ensure collaboration and consistency across the team and to provide subject matter expertise
• Act as a Source SME across OneStudyTeam as necessary

What You Bring to OneStudyTeam:

• 5+ years of relevant clinical research experience, including experience creating and/or QAing source document templates (CRFs)
• BA or BS, degree in business, science or related field, or AA degree and/or commensurate experience in relevant field(s)
• Prior experience owning successful execution of projects and/or teams, driving collaboration and successful completion, beyond an individual contributor status
• Experience working directly with clients (internal and/or external) and championing their long-term success
• Proven experience researching, learning, and utilizing new technologies and software
• Prior experience with a CTMS or other clinical research software tool is preferred
• Excellent communication (written and verbal), collaboration, and presentation skills
• Ability to thrive in a fast-paced, start-up environment - you are comfortable with ambiguity and find no job too big or small
• Extensive experience working with Excel 
• Excellent organizational skills, attention to detail, and critical and creative problem solving skills
• Solution-oriented thinking, a zest for learning, and a willingness to help whenever needed
• Excellent time managements skills and the ability to prioritize multiple workloads
• Familiarity with CLI (Command-Line Interface) is a plus
• Business-level fluency in English